Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs139231591 3 48342403 regulatory region variant C/T snv 1.2E-02 1
rs2280828 8 117750197 intergenic variant T/C snv 4.2E-02 1
rs4761669 12 94793846 intergenic variant T/G snv 0.27 1
rs73112098 5 67247451 regulatory region variant A/G snv 4.5E-02 1
rs75158213 3 48345739 intergenic variant T/C snv 1.2E-02 1
rs7640677 3 48340996 intergenic variant G/A snv 1.2E-02 1
rs1800452
CCR5AS ; CCR5
3 46373570 missense variant G/A snv 4.9E-03 1.9E-03 1
rs765009973
CCR5AS ; CCR5
3 46373909 missense variant G/T snv 7.4E-05 2.1E-05 1
rs2853699
CCR8
3 39332411 missense variant C/A;G;T snv 4.0E-06; 0.21; 2.8E-05 1
rs2907092
CTNND2
5 11047569 intron variant T/A;G snv 1
rs2586052
CUEDC1
17 57885718 5 prime UTR variant A/G;T snv 1
rs10025419
EMCN
4 100647799 intron variant G/A snv 0.87 1
rs2866233
EMCN
4 100649444 intron variant G/C;T snv 1
rs396716
FCGR3A
1 161544806 missense variant A/G snv 7.2E-05 6.3E-05 1
rs1552896
FREM1
9 14841389 intron variant C/A;G snv 1
rs4349147
IL32
16 3074919 intron variant A/G snv 0.69 1
rs3807044
KCNK16 ; LOC105375047
6 39322933 5 prime UTR variant C/T snv 0.37 1
rs6909587
LOC101928923 ; LOC105378072
6 155880114 intergenic variant C/T snv 0.78 1
rs11087114
MACROD2-AS1 ; MACROD2
20 14931037 intron variant G/A;C snv 1
rs9648724
PRKAG2 ; LOC644090
7 151805216 intron variant G/A snv 0.21 1
rs12587266
RIN3
14 92580298 intron variant A/G snv 0.63 1
rs6575267
RIN3
14 92580988 intron variant A/C snv 0.63 1
rs7154653
RIN3
14 92577033 intron variant T/A;C snv 1
rs113162402
SEPTIN4-AS1 ; SEPTIN4
17 58522103 splice acceptor variant T/A snv 1
rs1408270
SLC17A3
6 25872956 intron variant A/G snv 0.25 1